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FDA 510(k)

OptiCross 18, 30 MHz Peripheral Imaging Catheter

K-Number: K160514 · 2016-06-22

Decision Date2016-06-22
Product CodeOBJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OptiCross 18, 30 MHz Peripheral Imaging Catheter is a medical device manufactured by Boston Scientific Corporation. It received FDA 510(k) clearance on 2016-06-22 under approval number K160514. The device is classified under product code OBJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OptiCross 18, 30 MHz Peripheral Imaging Catheter?

OptiCross 18, 30 MHz Peripheral Imaging Catheter is a medical device that received FDA 510(k) clearance on 2016-06-22. It is manufactured by Boston Scientific Corporation. The 510(k) number is K160514.

When was OptiCross 18, 30 MHz Peripheral Imaging Catheter approved by the FDA?

OptiCross 18, 30 MHz Peripheral Imaging Catheter received FDA 510(k) clearance on 2016-06-22, under approval number K160514.

What company makes OptiCross 18, 30 MHz Peripheral Imaging Catheter?

OptiCross 18, 30 MHz Peripheral Imaging Catheter is manufactured by Boston Scientific Corporation.

What is the FDA product code for OptiCross 18, 30 MHz Peripheral Imaging Catheter?

The FDA product code for OptiCross 18, 30 MHz Peripheral Imaging Catheter is OBJ.

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Official Source

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